Evidence reported in the October issue of Cell Metabolism¹（新陈代谢） , a Cell Press publication, offers a completely new explanation for why people with diabetes² account for more than half of all patients requiring dialysis（透析） or kidney transplantation. It appears that insulin（胰岛素） has a significant influence on the structure and proper function of a particular group of very specialized³ cells, known as podocytes（肾小囊脏层细胞） , that are integral（完整的） to the kidney's ability to do its job filtering blood. "We've found that when you lose insulin signaling in the podocytes, the filter is not maintained," said Richard Coward of the University of Bristol. "Insulin action on the podocyte（足状突细胞） is really important to kidney function."

In the past, diabetic kidney failure had been considered a result of the toxic⁴ effects of high blood-sugar levels on cells of the kidney. That may still be true, Coward said, but the new findings suggest that insulin resistance of podocytes is key. He suggests that general insulin-sensitizing drugs or drugs specifically designed to restore insulin sensitivity to podocytes might offer new treatments for the most common cause of kidney failure in the world.

Podocytes are quite remarkable⁵ cells that look a lot like octopuses⁷（章鱼） , Coward explained. "They have a massive cell body with processes extending from them" like the legs of an octopus⁶. Those cells form a lace-like structure that is important to preventing albumin（白蛋白） proteins from leaking out of the bloodstream and into the urine. That leakage⁸ is used as an early sign of kidney disease, and it generally worsens over time.

The researchers had earlier shown that podocytes are uniquely sensitive to insulin. To find out what influence that insulin sensitivity might have on kidney function in the new study, they generated mice lacking insulin receptors only in their podocytes. Sure enough, those animals began to show protein in their urine along with other features characteristic of diabetic kidney disease. That was despite the fact that the animals weren't diabetic and had normal blood sugar levels.

Further examination found that insulin activity in podocytes causes them to remodel⁹ themselves. Coward said that makes sense in that podocytes "are not static cells. They move actively¹⁰ and contract or remodel themselves." He suspects that the cells do this in response to insulin because they need to "brace¹¹ themselves for an increased work load after a meal."

Coward said there is already some evidence that traditional insulin-sensitizing drugs can help protect against kidney disease in diabetic animals. Insulin sensitizers that specifically target the podocyte might be good treatments for preventing kidney failure, he said, especially given that very sensitive urine tests can now identify a breakdown¹² in the kidneys early.